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Harmonization of pipeline for preclinical multicenter plasma protein and miRNA biomarker discovery in a rat model of post-traumatic epileptogenesis

机译:临床前多中心血浆蛋白管道和小型创伤性癫痫发育大鼠模型中的临床前多中心血浆蛋白和miRNA生物标志物发现

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The Epilepsy Bioinformatics Study for Antiepileptogenic Therapy (EpiBioS4Rx) is an international, multicenter, multidisciplinary study aimed at preventing epileptogenesis (EpiBioS4Rx: https://epibios.loni.usc.edu/). One of the study's major objectives is the discovery of diagnostic, prognostic, and predictive plasma protein and microRNA (miRNA) biomarkers that are sensitive, specific, and translatable to the human condition. Epilepsy due to structural brain abnormalities, secondary to neurological insults such as traumatic brain injury (TBI), currently represents similar to 50% of all epilepsy cases. In the preclinical EpiBioS4Rx study, TBI was induced in adult male Sprague Dawley rats using a standardized protocol for lateral fluid-percussion injury. Whole blood was collected from the tail vein at baseline and 2, 9 and 30 days post-injury and processed for plasma separation. Biomaterial properties, sample preparation and integrity, and choice of analysis platform can significantly impact measured marker levels and, in turn, interpretation with respect to injury and/or other variables. We present here the results of procedural harmonization for the first 320 rats included in the EpiBioS4Rx study study, from three international research centers, and preliminary proteomic and miRNA analyses. We also discuss experimental considerations for establishing rigorous quality controls with the goal of harmonizing operating procedures across study sites, and delivering high-quality specimens for preclinical biomarker discovery in a rat model of post-traumatic epilepsy (PTE).
机译:癫痫素治疗的癫痫生物信息学研究(EPIBIOS4RX)是一种旨在预防癫痫发育的国际,多中心的多学科研究(EPIBIOS4RX:https://epibios.loni.usc.edu/)。该研究的主要目标之一是发现诊断,预后和预测性血浆蛋白和微小RONA(miRNA)生物标志物,其敏感,特异性和可与人体状况相比。由于结构脑异常,继发性脑损伤等创伤性脑损伤(TBI),目前代表与所有癫痫病例的50%相似。在临床前表皮治疗中的研究中,使用标准化方案用于横向流体冲击损伤的标准化方案,在成年雄性Sprague Dawley大鼠中诱导TBI。从损伤后的基线和2,9和30天的尾静脉收集全血,并处理血浆分离。生物材料性质,样品制备和完整性,以及分析平台的选择可以显着影响测量标记水平,然后反映出对损伤和/或其他变量的解释。我们在这里展示了综合症4RX研究研究中包含的前320只大鼠的程序协调结果,来自三个国际研究中心,初步蛋白质组学和miRNA分析。我们还讨论了建立严格质量控制的实验考虑因素,以实现跨学习网站的运营程序,并在创伤后癫痫(PTE)大鼠模型中提供高质量的临床前生物标志物发现。

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